Canonical Allele Identifier: CA1173563442
Gene: RPE65 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68444696A= , CM000663.2:g.68444696A= GRCh38
NC_000001.10:g.68910379A= , CM000663.1:g.68910379A= GRCh37
NC_000001.9:g.68682967A= NCBI36
NG_008472.1:g.10264T=
NG_008472.2:g.10264T=

Transcript Alleles

HGVS Amino-acid change
ENST00000262340.6:c.354-24T= MANE Select ENSP00000262340.5:n.354-24T=
ENST00000262340.5:c.354-24T= ENSP00000262340.5:n.354-24T=
NM_000329.2:c.354-24T= NP_000320.1:n.354-24T=
XM_017002027.1:c.78-24T= XP_016857516.1:n.78-24T=
NM_000329.3:c.354-24T= MANE Select NP_000320.1:n.354-24T=